Korkmaz Orhan Tansel, Saydam Faruk, Dalkiran Bahar, Değirmenci İrfan, Tunçel Neşe
Department of Physiology, Faculty of Medicine, Eskisehir Osmangazi University, 26040, Eskisehir, Turkey.
Department of Medical Biology, Medical Faculty, Recep Tayyip Erdogan University, 53100, Rize, Turkey.
Cell Biochem Biophys. 2025 Jun;83(2):1963-1972. doi: 10.1007/s12013-024-01606-0. Epub 2024 Nov 17.
Adipose tissue represents an organ that is highly dynamic and contributes toward vital survival events such as immune responses, lactation, metabolism fuel, and thermogenesis. Data emerging from recent studies support the notion of adipose tissue being organized into a complex system characterized by a discrete anatomy, elevated physiological plasticity, and specific vascular and nerve supplies. Vasoactive intestinal peptide (VIP), along with its receptors, type 1 (VPAC1) and type 2 (VPAC2), has been implicated in various physiological and pathophysiological processes. However, studies on VIP and its receptors in adipose tissue are limited. To explore VIP's presence and activity, as well as its adipose tissue-based receptors, we conducted a study on isolated adipocytes and adipose tissue from inguinal white adipose tissue (WAT) and interscapular brown adipose tissue (BAT) in normal and cold-stressed rats. Our findings indicate the presence of the gene expression VIP and VPAC1 in both WAT and BAT under normal conditions, while VPAC2 was absent. In both WAT and BAT, cold exposure upregulated VIP gene expression. However, the response of VIP receptors to cold exposure is controversial. VPAC2 gene expression was induced in both WAT and BAT, while VPAC1 gene expression presented no change of significance in BAT and a slight reduction in WAT. Additionally, VIP, VPAC1, and VPAC2 proteins were identified from Western blot studies on white and brown adipocytes. After exposure to cold there was an increase of significance in the VIP, VPAC1, and VPAC2 protein levels. This study provides novel insights into how VIP and its receptors alter gene expression and protein levels in adipose tissue and adipocytes during cold stress, indicating their potential involvement in adipose tissue regulation. The findings propose VIP's potentially crucial role in adipose tissue's adaptation to cold stress by affecting the metabolic and biochemical functions of subcutaneous and interscapular adipocytes, with potentially significant implications in the context of developing therapies targeting metabolic disorders.
脂肪组织是一个高度动态的器官,对免疫反应、泌乳、代谢燃料和产热等重要的生存活动有重要作用。最近研究得出的数据支持了脂肪组织被组织成一个复杂系统的观点,该系统具有离散的解剖结构、较高的生理可塑性以及特定的血管和神经供应。血管活性肠肽(VIP)及其1型受体(VPAC1)和2型受体(VPAC2)参与了各种生理和病理生理过程。然而,关于VIP及其受体在脂肪组织中的研究有限。为了探究VIP的存在和活性及其在脂肪组织中的受体,我们对正常和冷应激大鼠腹股沟白色脂肪组织(WAT)和肩胛间棕色脂肪组织(BAT)分离出的脂肪细胞和脂肪组织进行了研究。我们的研究结果表明,在正常条件下,WAT和BAT中均存在VIP和VPAC1的基因表达,而VPAC2不存在。在WAT和BAT中,冷暴露均上调了VIP基因表达。然而,VIP受体对冷暴露的反应存在争议。WAT和BAT中均诱导了VPAC2基因表达,而BAT中VPAC1基因表达无显著变化,WAT中则略有降低。此外,通过对白色和棕色脂肪细胞的蛋白质印迹研究鉴定出了VIP、VPAC1和VPAC2蛋白。冷暴露后,VIP、VPAC1和VPAC2蛋白水平显著增加。这项研究为冷应激期间VIP及其受体如何改变脂肪组织和脂肪细胞中的基因表达和蛋白质水平提供了新的见解,表明它们可能参与脂肪组织调节。研究结果表明,VIP可能通过影响皮下和肩胛间脂肪细胞的代谢和生化功能,在脂肪组织适应冷应激中发挥关键作用,这对于开发针对代谢紊乱的治疗方法可能具有重要意义。